{"id":26,"date":"2020-12-02T10:36:47","date_gmt":"2020-12-02T09:36:47","guid":{"rendered":"http:\/\/gawel.edu.pl\/?page_id=26"},"modified":"2026-03-03T17:07:52","modified_gmt":"2026-03-03T16:07:52","slug":"publications","status":"publish","type":"page","link":"https:\/\/gawel.edu.pl\/index.php\/publications\/","title":{"rendered":"Publications"},"content":{"rendered":"\n<ol reversed class=\"wp-block-list\">\n<li style=\"font-size:16px\">A. Pareek, M. Morawiak, E. Masoumifeshani, P. Gawe\u0142, <a href=\"https:\/\/doi.org\/10.1021\/acs.joc.5c02906\" data-type=\"link\" data-id=\"https:\/\/doi.org\/10.1021\/acs.joc.5c02906\" target=\"_blank\" rel=\"noreferrer noopener\"><em>The Journal of Organic Chemistry<\/em> <strong>2026<\/strong>, <em>91<\/em>, 2837\u20132843<\/a>. Photostable\u202f\u03c0-Expanded Furans via Base-Mediated Quinone\u202fOxygen-Annulation.<\/li>\n\n\n\n<li style=\"font-size:16px\">V. Sharma, P. Bartos, M. Morawiak, P. Gawe\u0142, <a href=\"https:\/\/doi.org\/10.1021\/acs.joc.5c02409\" target=\"_blank\" rel=\"noreferrer noopener\"><em>The Journal of Organic Chemistry<\/em> <strong>2026<\/strong>, 91, 1842\u20131847<\/a> Acid-Mediated Dimerization of TIPS-Pentacene.<\/li>\n\n\n\n<li style=\"font-size:16px\">A. Pareek, Y. Qiu, M. A. Johnson, R. Tykwinski, P. Gawe\u0142, <a href=\"https:\/\/doi.org\/10.1039\/D5SC04462F\" data-type=\"link\" data-id=\"https:\/\/doi.org\/10.1039\/D5SC04462F\" target=\"_blank\" rel=\"noreferrer noopener\"><em>Chemical Science<\/em> <strong>2026<\/strong>, <em>17<\/em>, 791-830<\/a>. The Versatile World of Cumulene Chemistry.<\/li>\n\n\n\n<li style=\"font-size:16px\">N. Dutkiewicz, M. Majdecki, B. Golec, I. Wielgus, P. Gawe\u0142, A. Gorski, <a href=\"https:\/\/doi.org\/10.1002\/chem.202502331\" data-type=\"link\" data-id=\"https:\/\/doi.org\/10.1002\/chem.202502331\" target=\"_blank\" rel=\"noreferrer noopener\"><em>Chemistry \u2013 A European Journal<\/em>, <strong>2025<\/strong>, <em>31<\/em>, e02331<\/a>. Porphyrin\u2013Acene Dyads for Controlled Singlet Oxygen Generation and Depletion.<\/li>\n\n\n\n<li style=\"font-size:16px\">A. Tyszka-Gumkowska, M. Brzezi\u0144ski, S. Gawinkowski, T. Polczyk, W. Wegner, M. Wlaz\u0142o, P. Bernatowicz, J. Nawrocki, P. Gawe\u0142, K. Noworyta, J. Ostapko, <a href=\"https:\/\/doi.org\/10.1021\/acs.chemmater.5c01951\" data-type=\"link\" data-id=\"https:\/\/doi.org\/10.1021\/acs.chemmater.5c01951\" target=\"_blank\" rel=\"noreferrer noopener\"><em>Chemistry of Materials<\/em> <strong>2025<\/strong>,&nbsp;37, 8048\u20138058<\/a>. Reductive Transformation of Imine Covalent Organic Frameworks into Emissive Polymers: Insights into Emission Quenching.<\/li>\n\n\n\n<li style=\"font-size:16px\">P. Baronas, J. Lekavi\u010dius, M. Majdecki, J. L. Elholm, K. Kazlauskas, P. Gawe\u0142, K. Moth-Poulsen,  <a href=\"https:\/\/doi.org\/10.1021\/acscentsci.4c02059\" data-type=\"link\" data-id=\"https:\/\/doi.org\/10.1021\/acscentsci.4c02059\" target=\"_blank\" rel=\"noreferrer noopener\"><em>ACS Central Science<\/em> <strong>2025, <\/strong><em>11<\/em>, 413\u2013421. <\/a> Automated Research Platform for Development of Triplet\u2013Triplet Annihilation Photon Upconversion Systems.<\/li>\n\n\n\n<li style=\"font-size:16px\">A. Pareek, M. Y. Mehboob, M. Cieplak, M. Majdecki, H. Szabat, K. Noworyta, P. Po\u0142czy\u0144ski, M. Morawiak, P. S. Sharma, C. Foroutan-Nejad, P. Gawe\u0142, <a href=\"https:\/\/doi.org\/10.1021\/jacs.4c16189\" data-type=\"link\" data-id=\"https:\/\/doi.org\/10.1021\/jacs.4c16189\" target=\"_blank\" rel=\"noreferrer noopener\"><em>Journal of the American Chemical Society<\/em> <strong>2025<\/strong>, <em>147<\/em>, 5996-6005<\/a>. Indoloindolizines: The Complete Story of a Polycyclic Aromatic Scaffold from Theoretical Design to Organic Field-Effect Transistor Applications.<em> <\/em><br><em><strong>Highlighted in:<\/strong><\/em><br>\u03c0-Extended Indoloindolizine: A New Semiconducting Module. <a href=\"https:\/\/doi.org\/10.1055\/a-2558-0174\" data-type=\"link\" data-id=\"https:\/\/doi.org\/10.1055\/a-2558-0174\" target=\"_blank\" rel=\"noreferrer noopener\">Synfacts 2025, 21 (05), 464-464<\/a><br>Naukowcy opracowali now\u0105 koncepcj\u0119 projektowania p\u00f3\u0142przewodnik\u00f3w organicznych, <a href=\"https:\/\/scienceinpoland.pl\/aktualnosci\/news%2C106224%2Cnaukowcy-opracowali-nowa-koncepcje-projektowania-polprzewodnikow\" data-type=\"link\" data-id=\"https:\/\/scienceinpoland.pl\/aktualnosci\/news%2C106224%2Cnaukowcy-opracowali-nowa-koncepcje-projektowania-polprzewodnikow\" target=\"_blank\" rel=\"noreferrer noopener\">Nauka w Polsce<\/a>, PAP<br>Polski prze\u0142om w produkcji p\u00f3\u0142przewodnik\u00f3w organicznych, <a href=\"https:\/\/www.youtube.com\/watch?v=B4jS9dZ_w7E\" data-type=\"link\" data-id=\"https:\/\/www.youtube.com\/watch?v=B4jS9dZ_w7E\" target=\"_blank\" rel=\"noreferrer noopener\">Blog Techniczny<\/a>, Komputer \u015awiat<\/li>\n\n\n\n<li style=\"font-size:16px\">M. Majdecki, C.-H. Hsu, C.-H. Wang, E. H.-C. Shi, M. Zakrocka, Y.-C. Wei, B.-H. Chen, C.-H. Lu, S.-D. Yang, P.-T. Chou, P. Gawe\u0142, <a href=\"https:\/\/onlinelibrary.wiley.com\/doi\/10.1002\/anie.202401103\" target=\"_blank\" rel=\"noreferrer noopener\"><em>Angewandte Chemie International Edition<\/em>, <strong>2024<\/strong>,&nbsp;<em>63<\/em>, e202401103<\/a> Singlet Fission in a New Series of Systematically Designed Through-space Coupled Tetracene Oligomers.<br><em><strong>Highlighted in:<\/strong><\/em><br>Molekularni krawcy uszyli nano\u015bnie\u017cynki dla wydajniejszych ogniw s\u0142onecznych, <a href=\"https:\/\/naukawpolsce.pl\/aktualnosci\/news%2C101656%2Cmolekularni-krawcy-uszyli-nanosniezynki-dla-wydajniejszych-ogniw\" data-type=\"link\" data-id=\"https:\/\/naukawpolsce.pl\/aktualnosci\/news%2C101656%2Cmolekularni-krawcy-uszyli-nanosniezynki-dla-wydajniejszych-ogniw\" target=\"_blank\" rel=\"noreferrer noopener\">Nauka w Polsce<\/a>, PAP<br>Behind the Science: Singlet Fission in a New Series of Tetracene Oligomers, <a href=\"https:\/\/www.chemistryviews.org\/behind-the-science-singlet-fission-in-a-new-series-of-tetracene-oligomers\/\" data-type=\"link\" data-id=\"https:\/\/www.chemistryviews.org\/behind-the-science-singlet-fission-in-a-new-series-of-tetracene-oligomers\/\" target=\"_blank\" rel=\"noreferrer noopener\">ChemistryViews<\/a><\/li>\n\n\n\n<li style=\"font-size:16px\">P Gawe\u0142, C. Foroutan-Nejad, <a href=\"https:\/\/rdcu.be\/dsob1\" target=\"_blank\" rel=\"noreferrer noopener\"><em>Nature<\/em>, <strong>2023<\/strong>, <em>623<\/em>,  922-923<\/a>. Carbon rings push limits of chemical theories.<\/li>\n\n\n\n<li style=\"font-size:16px\">C. W. Patrick, J. F. Woods, P. Gawel, C. E. Otteson, A. L. Thompson, T. D. W. Claridge, R. Jasti, H. L. Anderson, <a href=\"https:\/\/onlinelibrary.wiley.com\/doi\/10.1002\/anie.202116897\" target=\"_blank\" rel=\"noreferrer noopener\"><em>Angewandte Chemie International Edition<\/em> <strong>2022<\/strong>,&nbsp;<em>61<\/em>, e202116897<\/a> Polyyne [3]rotaxanes: Synthesis via dicobalt carbonyl complexes and enhanced stability.<\/li>\n\n\n\n<li style=\"font-size:16px\">P. Gawel, S. Woltering, Y. Xiong, K. Christensen, H. L. Anderson, <a rel=\"noreferrer noopener\" href=\"https:\/\/onlinelibrary.wiley.com\/doi\/abs\/10.1002\/anie.202013623\" target=\"_blank\"><em>Angewandte Chemie International Edition<\/em>, <strong>2021<\/strong>, <em>60<\/em>, 5941-59471<\/a>. Masked Alkyne Equivalents for the Synthesis of Mechanically Interlocked Polyynes.<\/li>\n\n\n\n<li style=\"font-size:16px\">S. L. Woltering, P. Gawel, K. E. Christensen, A. L. Thompson, H. L. Anderson, <a rel=\"noreferrer noopener\" href=\"https:\/\/pubs.acs.org\/doi\/abs\/10.1021\/jacs.0c05308\" target=\"_blank\"><em>Journal of the American Chemical Society<\/em> <strong>2020<\/strong>, <em>142<\/em>, 13523-13532<\/a>. Photochemical Unmasking of Polyyne Rotaxanes.<\/li>\n\n\n\n<li style=\"font-size:16px\">L. M. Scriven, K. Kaiser, F. Schulz, A. J. Sterling, S. L. Woltering, P. Gawel, K. E. Christensen, H. L. Anderson, L. Gross, <a rel=\"noreferrer noopener\" href=\"https:\/\/pubs.acs.org\/doi\/abs\/10.1021\/jacs.0c05033\" target=\"_blank\"><em>Journal of the American Chemical Society<\/em> <strong>2020<\/strong>, <em>142<\/em>, 12921-12924<\/a>. Synthesis of Cyclo[18]carbon via Debromination of C<sub>18<\/sub>Br<sub>6<\/sub>.<\/li>\n\n\n\n<li style=\"font-size:16px\">K. Kaiser, L. M. Scriven, F. Schulz, P. Gawel,* L. Gross, H. L. Anderson, <a rel=\"noreferrer noopener\" href=\"https:\/\/science.sciencemag.org\/content\/365\/6459\/1299.abstract\" target=\"_blank\"><em>Science<\/em> <strong>2019<\/strong>, <em>365<\/em>, 1299-1301<\/a>. An sp-hybridized molecular carbon allotrope, cyclo[18]carbon.<\/li>\n\n\n\n<li style=\"font-size:16px\">N. Pavli\u010dek, P. Gawel,* D. R. Kohn, Z. Majzik, Y. Xiong, G. Meyer, H. L. Anderson, L. Gross, <a rel=\"noreferrer noopener\" href=\"https:\/\/www.nature.com\/articles\/s41557-018-0067-y\" target=\"_blank\"><em>Nature Chemistry<\/em> <strong>2018<\/strong>, <em>10<\/em>, 853-858<\/a>. Polyyne formation via skeletal rearrangement induced by atomic manipulation.<\/li>\n\n\n\n<li style=\"font-size:16px\">D. R. Kohn, P. Gawel, Y. Xiong, K. E. Christensen, H. L. Anderson, <a rel=\"noreferrer noopener\" href=\"https:\/\/pubs.acs.org\/doi\/abs\/10.1021\/acs.joc.7b03015\" target=\"_blank\"><em>The Journal of Organic Chemistry<\/em> <strong>2018<\/strong>, <em>83<\/em>, 2077-2086<\/a>. Synthesis of Polyynes Using Dicobalt Masking Groups.<\/li>\n\n\n\n<li style=\"font-size:16px\">N. Kerisit, P. Gawel, B. Levandowski, Y. F. Yang, V. Garc\u00eda\u2010L\u00f3pez, N. Trapp, L. Ruhlmann, C. Boudon, K. N. Houk, F. Diederich, <a rel=\"noreferrer noopener\" href=\"https:\/\/chemistry-europe.onlinelibrary.wiley.com\/doi\/abs\/10.1002\/chem.201703903\" target=\"_blank\"><em>Chemistry \u2013 A European Journal<\/em> <strong>2018<\/strong>, <em>24<\/em>, 159-168<\/a>. A Four\u2010Step Synthesis of Substituted 5,11\u2010Dicyano\u20106,12\u2010diaryltetracenes with Enhanced Stability and High Fluorescence Emission.<\/li>\n\n\n\n<li style=\"font-size:16px\">S. Haberland, A. D. Finke, N. Kerisit, C. Katan, Y. Trolez, P. Gawel, I. Leito, M. L\u00f5kov, R. J\u00e4rviste, K. Kaupmees, N. Trapp, L. Ruhlmann, C. Boudon, D. Himmel, F. Diederich, <a rel=\"noreferrer noopener\" href=\"https:\/\/chemistry-europe.onlinelibrary.wiley.com\/doi\/abs\/10.1002\/ejoc.201800039\" target=\"_blank\"><em>European Journal of Organic Chemistry<\/em> <strong>2018<\/strong>, 739-749<\/a>. Enhancement of Push\u2013Pull Properties of Pentafulvene and Pentafulvalene Derivatives by Protonation at Carbon.<\/li>\n\n\n\n<li style=\"font-size:16px\">E. A. Margulies, N. Kerisit, P. Gawel, C. M. Mauck, L. Ma, C. E. Miller, R. M. Young, N. Trapp, Y.-L. Wu, F. Diederich, M. R. Wasielewski, <a rel=\"noreferrer noopener\" href=\"https:\/\/pubs.acs.org\/doi\/abs\/10.1021\/acs.jpcc.7b07870\" target=\"_blank\"><em>The Journal of Physical Chemistry C<\/em> <strong>2017<\/strong>, <em>121<\/em>, 21262-21271<\/a>. Substituent Effects on Singlet Exciton Fission in Polycrystalline Thin Films of Cyano-Substituted Diaryltetracenes.<\/li>\n\n\n\n<li style=\"font-size:16px\">A. Khadria, Y. de Coene, P. Gawel, C. Roche, K. Clays, H. L. Anderson, <a rel=\"noreferrer noopener\" href=\"https:\/\/pubs.rsc.org\/en\/content\/articlelanding\/2017\/ob\/c6ob02319c\/unauth#!divAbstract\" target=\"_blank\"><em>Organic &amp; Biomolecular Chemistry<\/em> <strong>2017<\/strong>, <em>15<\/em>, 947-956<\/a>. Push\u2013pull pyropheophorbides for nonlinear optical imaging.<\/li>\n\n\n\n<li style=\"font-size:16px\">P. Gawel, E. A. Halabi, D. Schweinfurth, N. Trapp, L. Ruhlmann, C. Boudon, F. Diederich, <a rel=\"noreferrer noopener\" href=\"https:\/\/chemistry-europe.onlinelibrary.wiley.com\/doi\/abs\/10.1002\/ejoc.201600470\" target=\"_blank\"><em>European Journal of Organic Chemistry<\/em> <strong>2016<\/strong>, 2919-2924<\/a>. Synthesis of Dicyano\u2010Substituted Benzo[c]fluorenes from Tetraaryl[3]cumulenes.<\/li>\n\n\n\n<li style=\"font-size:16px\">C. Dengiz, C. Prange, P. Gawel, N. Trapp, L. Ruhlmann, C. Boudon, F. Diederich, <a rel=\"noreferrer noopener\" href=\"https:\/\/www.sciencedirect.com\/science\/article\/abs\/pii\/S0040402016300175\" target=\"_blank\"><em>Tetrahedron<\/em> <strong>2016<\/strong>, <em>72<\/em>, 1213-1224<\/a>. Push\u2013pull chromophores by reaction of 2,3,5,6-tetrahalo-1,4-benzoquinones with 4-(<em>N,N<\/em>-dialkylanilino)acetylenes.<\/li>\n\n\n\n<li style=\"font-size:16px\">E. A. Margulies, Y.-L. Wu, P. Gawel, S. A. Miller, L. E. Shoer, R. D. Schaller, F. Diederich, M. R. Wasielewski, <a rel=\"noreferrer noopener\" href=\"https:\/\/onlinelibrary.wiley.com\/doi\/abs\/10.1002\/ange.201501355\" target=\"_blank\"><em>Angewandte Chemie International Edition<\/em> <strong>2015<\/strong>, <em>54<\/em>, 8679-8683<\/a>. Sub\u2010Picosecond Singlet Exciton Fission in Cyano\u2010Substituted Diaryltetracenes.<\/li>\n\n\n\n<li style=\"font-size:16px\">P. Gawel, Y.-L. Wu, A. D. Finke, N. Trapp, M. Zalibera, C. Boudon, J.-P. Gisselbrecht, W. B. Schweizer, G. Gescheidt, F. Diederich, <a rel=\"noreferrer noopener\" href=\"https:\/\/chemistry-europe.onlinelibrary.wiley.com\/doi\/abs\/10.1002\/chem.201406583\" target=\"_blank\"><em>Chemistry \u2013 A European Journal<\/em> <strong>2015<\/strong>, <em>21<\/em>, 6215-6225<\/a>. Push\u2013Pull Buta\u20101,2,3\u2010trienes: Exceptionally Low Rotational Barriers of Cumulenic C=C Bonds and Proacetylenic Reactivity.<\/li>\n\n\n\n<li style=\"font-size:16px\">P. Gawel, C. Dengiz, A. D. Finke, N. Trapp, C. Boudon, J.-P. Gisselbrecht, F. Diederich, <a rel=\"noreferrer noopener\" href=\"https:\/\/onlinelibrary.wiley.com\/doi\/abs\/10.1002\/anie.201402299\" target=\"_blank\"><em>Angewandte Chemie International Edition<\/em> <strong>2014<\/strong>, <em>53<\/em>, 4341-4345.<\/a> Synthesis of Cyano\u2010Substituted Diaryltetracenes from Tetraaryl[3]cumulenes.<\/li>\n\n\n\n<li style=\"font-size:16px\">H. Dodziuk, V. Vetokhina, H. Hopf, R. Luboradzki, P. Gawel, J. Waluk, <a rel=\"noreferrer noopener\" href=\"https:\/\/aip.scitation.org\/doi\/abs\/10.1063\/1.3683454\" target=\"_blank\"><em>The Journal of Chemical Physics<\/em> <strong>2012<\/strong>, <em>136<\/em>, 074201-074209<\/a>. Electronic states of cyclophanes with small bridges.<\/li>\n\n\n\n<li style=\"font-size:16px\">T. Bauer, S. Smolinski, P. Gawel, J. Jurczak, <a rel=\"noreferrer noopener\" href=\"https:\/\/www.sciencedirect.com\/science\/article\/abs\/pii\/S0040403911011543\" target=\"_blank\"><em>Tetrahedron Letters<\/em> <strong>2011<\/strong>, <em>52<\/em>, 4882-4884<\/a>. Enantioselective addition of phenylacetylene to aldehydes catalyzed by a&nbsp;d-glucosamine-derived sulfonamide\u2013titanium complex.<\/li>\n<\/ol>\n\n\n\n<p><\/p>\n","protected":false},"excerpt":{"rendered":"","protected":false},"author":1,"featured_media":0,"parent":0,"menu_order":3,"comment_status":"closed","ping_status":"closed","template":"templates\/template-full-width.php","meta":{"footnotes":""},"class_list":["post-26","page","type-page","status-publish","hentry"],"_links":{"self":[{"href":"https:\/\/gawel.edu.pl\/index.php\/wp-json\/wp\/v2\/pages\/26","targetHints":{"allow":["GET"]}}],"collection":[{"href":"https:\/\/gawel.edu.pl\/index.php\/wp-json\/wp\/v2\/pages"}],"about":[{"href":"https:\/\/gawel.edu.pl\/index.php\/wp-json\/wp\/v2\/types\/page"}],"author":[{"embeddable":true,"href":"https:\/\/gawel.edu.pl\/index.php\/wp-json\/wp\/v2\/users\/1"}],"replies":[{"embeddable":true,"href":"https:\/\/gawel.edu.pl\/index.php\/wp-json\/wp\/v2\/comments?post=26"}],"version-history":[{"count":46,"href":"https:\/\/gawel.edu.pl\/index.php\/wp-json\/wp\/v2\/pages\/26\/revisions"}],"predecessor-version":[{"id":36463,"href":"https:\/\/gawel.edu.pl\/index.php\/wp-json\/wp\/v2\/pages\/26\/revisions\/36463"}],"wp:attachment":[{"href":"https:\/\/gawel.edu.pl\/index.php\/wp-json\/wp\/v2\/media?parent=26"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}